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腺病毒2型的主要晚期启动子可被RNA聚合酶IIO、IIA和IIB精确转录。

The major late promoter of adenovirus-2 is accurately transcribed by RNA polymerases IIO, IIA, and IIB.

作者信息

Kim W Y, Dahmus M E

机构信息

Department of Biochemistry and Biophysics, University of California, Davis 95616.

出版信息

J Biol Chem. 1989 Feb 25;264(6):3169-76.

PMID:2914948
Abstract

Subunit IIa of mammalian RNA polymerase II contains at its C terminus 52 tandem repeats of the consensus sequence Tyr-Ser-Pro-Thr-Ser-Pro-Ser. This domain is unmodified in RNA polymerase IIA, extensively phosphorylated in RNA polymerase IIO, and absent from RNA polymerase IIB. In an effort to define the role of the C-terminal domain, we have measured the transcriptional activity of purified RNA polymerases IIO, IIA, and IIB. The ability of each polymerase subspecies to transcribe the major late promoter of adenovirus-2 was examined in a polymerase-dependent transcription system reconstituted from partially purified transcription factors. RNA polymerases IIO, IIA, and IIB are all capable of initiating specific transcripts from this promoter. The transcriptional activity was determined as a function of the concentration of RNA polymerase II, template DNA, and each of the essential general transcription factors. The transcriptional activities of RNA polymerases IIA and IIB were comparable and consistently greater than that of RNA polymerase IIO when assayed under the conditions described here. The kinetics of transcript formation is similar except that RNA polymerase IIO has a more pronounced lag. These results show that the C-terminal domain of subunit IIa is not essential for the accurate initiation of transcripts from the major late promoter of adenovirus-2 and that the effect of the C-terminal domain is not likely mediated by the general transcription factors required for the expression of class II genes.

摘要

哺乳动物RNA聚合酶II的亚基IIa在其C末端含有52个串联重复的共有序列Tyr-Ser-Pro-Thr-Ser-Pro-Ser。该结构域在RNA聚合酶IIA中未被修饰,在RNA聚合酶IIO中被广泛磷酸化,而在RNA聚合酶IIB中不存在。为了确定C末端结构域的作用,我们测量了纯化的RNA聚合酶IIO、IIA和IIB的转录活性。在由部分纯化的转录因子重构的聚合酶依赖性转录系统中,检测了每种聚合酶亚类转录腺病毒2主要晚期启动子的能力。RNA聚合酶IIO、IIA和IIB都能够从该启动子起始特异性转录本。转录活性被确定为RNA聚合酶II、模板DNA和每种必需的通用转录因子浓度的函数。在此处所述条件下进行测定时,RNA聚合酶IIA和IIB的转录活性相当,并且始终大于RNA聚合酶IIO的转录活性。转录本形成的动力学相似,只是RNA聚合酶IIO有更明显的延迟。这些结果表明,亚基IIa的C末端结构域对于从腺病毒2主要晚期启动子准确起始转录本不是必需的,并且C末端结构域的作用不太可能由II类基因表达所需的通用转录因子介导。

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